Literature DB >> 22005610

Synthetic matrices to serve as niches for muscle cell transplantation.

Sarah Fernandes1, Shannon Kuklok, Joe McGonigle, Hans Reinecke, Charles E Murry.   

Abstract

Poor cell retention and limited cell survival after grafting are major limitations of cell therapy. Recent studies showed that the use of matrices as vehicles at the time of cell injection can significantly improve cell engraftment by providing an appropriate structure and physical support for the injected cells. Properly designed matrices can also promote the organization of the cells into a functioning cardiac-like tissue and enhance integration between the host and the engrafted tissue. Furthermore, the use of an injectable biomaterial provides an opportunity to release in situ bioactive molecules that can further enhance the beneficial effects of cell transplantation. In this article we review a large variety of biologically derived synthetic and hybrid materials that have been tested as matrices for cardiac repair. We summarize the optimal parameters required for an ideal matrix including biocompatibility, injectability, degradation rate, and mechanical properties. Using an in vivo subcutaneous grafting model, we also provide novel data involving a side-by-side comparison of six synthetic matrices derived from maltodextrin. By systematically varying polymer molecular weight, cross-link density, and availability of cell adhesion motifs, a synthetic matrix was identified that supported skeletal myotube formation similar to Matrigel™. Our results emphasize not only the need to have a range of tunable matrices for cardiac cell therapy but also the importance of further characterizing the physical properties required for an ideal injectable matrix.
Copyright © 2011 S. Karger AG, Basel.

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Year:  2011        PMID: 22005610      PMCID: PMC3697876          DOI: 10.1159/000331414

Source DB:  PubMed          Journal:  Cells Tissues Organs        ISSN: 1422-6405            Impact factor:   2.481


  59 in total

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7.  Self-assembling peptide nanofibers and skeletal myoblast transplantation in infarcted myocardium.

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8.  Absence of regeneration in the MRL/MpJ mouse heart following infarction or cryoinjury.

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9.  Delivering stem cells to the heart in a collagen matrix reduces relocation of cells to other organs as assessed by nanoparticle technology.

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10.  Extracellular matrix formation after transplantation of human embryonic stem cell-derived cardiomyocytes.

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Journal:  Cell Mol Life Sci       Date:  2009-10-22       Impact factor: 9.261

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  6 in total

1.  Parthenogenetic stem cells for tissue-engineered heart repair.

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5.  Myocardial repair of bioengineered cardiac patches with decellularized placental scaffold and human-induced pluripotent stem cells in a rat model of myocardial infarction.

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Review 6.  Engineering muscle tissue for the fetus: getting ready for a strong life.

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  6 in total

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